Treffer 1 - 20 von 21 für Suche 'SZABO, STEPHANIE D', Suchdauer: 1,97s Treffer weiter einschränken
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    A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population von Healey, Sue, Loud, Jennifer T, dos Santos Silva, Isabel, Hakonarson, Hakon, Garber, Judy, Blank, Stephanie V, Huzarski, Tomasz, Godwin, Andrew K, Spurdle, Amanda B, Soucy, Penny, Izatt, Louise, Southey, Melissa, Blum, Joanne L, Cox, Angela, Buys, Saundra S, Fasching, Peter A, Laitman, Yael, Rantala, Johanna, Peto, Julian, Montagna, Marco, Flesch-Janys, Dieter, Offit, Kenneth, Peock, Susan, Manoukian, Siranoush, Neuhausen, Susan L, Weitzel, Jeffrey, Wappenschmidt, Barbara, Sutter, Christian, Osorio, Ana, Rookus, Matti A, Terry, Mary-Beth, Friedman, Eitan, Ghoussaini, Maya, Martin, Nicholas G, Giraud, Sophie, Devilee, Peter, Gayther, Simon A, Engel, Christoph, Tung, Nadine, Singer, Christian F, Simard, Jacques, Byrski, Tomasz, Peterlongo, Paolo, Cook, Margaret, Bonanni, Bernardo, Goldgar, David E, Frost, Debra, Easton, Douglas F, Hoogerbrugge, Nicoline, Meindl, Alfons, Diasio, Robert B, Sinilnikova, Olga M, Kartsonaki, Christiana, Antoniou, Antonis C, Stoppa-Lyonnet, Dominique, Rodriguez, Gustavo C, Nathanson, Katherine L, Gaudet, Mia M, Cross, Simon S, Cybulski, Cezary, Winqvist, Robert, Fountzilas, George, van den Ouweland, Ans, Hansen, Thomas V O, Beattie, Mary S, Nielsen, Finn C, Douglas, Fiona, Caldes, Trinidad, Hopper, John L, Hogervorst, Frans B L, Oliver, Clare, Gerty, Sue M, Yannoukakos, Drakoulis, Lambrechts, Diether, Caron, Olivier, Lee, Adam M, Hardouin, Agnès, Vachon, Celine, Chenevix-Trench, Georgia, Holland, Helene, Blanco, Ignacio, Beckmann, Matthias W, Paridaens, Robert, Barrowdale, Daniel, Piedmonte, Marion, Couch, Fergus J, Lasset, Christine, Górski, Bohdan, Domchek, Susan M, Loman, Niklas, Nevanlinna, Heli, Rebbeck, Timothy, Thomassen, Mads, Narod, Stephen, Eccles, Diana, Benitez, Javier, Arason, Adalgeir, Basil, Jack, Lazaro, Conxi, Phelan, Catherine

    Veröffentlicht in Nature genetics

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    Expanding SPTAN1 monoallelic variant associated disorders: From epileptic encephalopathy to pure spastic paraplegia and ataxia von Morsy, Heba, Benkirane, Mehdi, Cali, Elisa, Zhelcheska, Kristina, Cipriani, Valentina, Galanaki, Evangelia, Maroofian, Reza, Efthymiou, Stephanie, Murphy, David, Banka, Siddharth, Clayton-Smith, Jill, Redman, Melody, Bassetti, Jennifer A., Nizon, Mathilde, Jamra, Rami Abu, Heruth, Marion, Krey, Ilona, Gburek-Augustat, Janina, Wieczorek, Dagmar, Mcentagart, Meriel, Goldenberg, Alice, Guyant-Marechal, Lucie, Garcia-Moreno, Hector, Giunti, Paola, Chabrol, Brigitte, Bacrot, Severine, Buissonnière, Roger, Gowda, Vykuntaraju K., Srinivasan, Varunvenkat M., Melegh, Béla, Szabó, András, Sümegi, Katalin, Cossée, Mireille, Ziff, Monica, Butterfield, Russell, Hunt, David, Hanna, Michael, Koenig, Michel, Vandrovcova, Jana, Houlden, Henry, Arumugam, P., Baple, E.L., Bleda, M., Boardman-Pretty, F., Boissiere, J.M., Boustred, C.R., Brittain, H., Caulfield, M.J., Chan, G.C., Daugherty, L.C., Devereau, A., Foulger, R.E., Fowler, T., Furió-Tarí, P., Halai, D., Hamblin, A., Henderson, S., Holman, J.E., Hubbard, T.J.P., Ibáñez, K., Jackson, R., Jones, L.J., Kasperaviciute, D., Lahnstein, L., Leigh, S.E.A., Leong, I.U.S., Lopez, F.J., Maleady-Crowe, F., Mason, J., McDonagh, E.M., Moutsianas, L., Mueller, M., Murugaesu, N., Odhams, C.A., Patch, C., Perez-Gil, D., Pullinger, J., Rahim, T., Riesgo-Ferreiro, P., Rogers, T., Ryten, M., Savage, K., Scott, R.H., Siddiq, A., Sieghart, A., Smedley, D., Smith, K.R., Sosinsky, A., Stevens, H.E., Stuckey, A., Sultana, R., Thompson, S.R., Tucci, A., Walsh, E., Watters, S.A., Welland, M.J., Williams, E., Witkowska, K., Wood, S.M., Zarowiecki, M.

    Veröffentlicht in Genetics in medicine

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